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Can a Light-Up face mask smooth wrinkles at home?

NCT ID NCT07054710

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study tested a device that uses red, infrared, and blue LED light plus vibration to improve skin health. 115 adults aged 35-65 used the device daily for 12 weeks. Researchers measured changes in fine lines, wrinkles, skin tone, and firmness using expert grading and imaging.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
LED light and vibration device
What this could lead to
If successful, this device could offer a convenient at-home option for improving skin appearance like fine lines and firmness.
What could go wrong
This is a small, completed study without a control group, so results may not be generalizable. Skin improvements are subjective and may vary.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

115 people

The number who actually took part.

Started

May 2025

Finished

Sep 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

35 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Subject is female or male (approximately 90% female and 10% male) * Subject is between the ages of 35-65 * Male subjects agree to remove all facial hair 24-48 hours prior to each visit and remain clean shaven daily throughout the study * Subject is of any Fitzpatrick (at least one of each, to be recorded) * Subject is of any of the following (Caucasian, African American, Asian, Hispanic) (at least one of each, to be recorded) * Subject has Self-Perceived Sensitive skin or Self-Perceived Non-Sensitive skin (approximately 50% sensitive and 50% non-sensitive) * Subject has the following on face (mild or greater): Fine lines, ≥3 on 10-point scale Wrinkles, ≥3 on 10-point scale Dull skin, ≥3 on 10-point scale Sagging, ≥3 on 10-point scale Uneven skin tone Roughness/texture At least one dark spot * Subject agrees to return all used and unused test materials at the end of the study * Subjects will use their regular SPF product or will use an SPF product provided by the Sponsor (if they do not have an SPF product) and practice sun safe practices for the duration of the study (Hat, sunglasses, etc.) * Subject agrees not to introduce any new cosmetic or toiletry products during the study other than the products provided in this study * Subject is willing to use a cosmetic device on their face * Subject is dependable and able to follow directions as outlined in the protocol and anticipates being available for all study visits * Subject is willing to participate in all study evaluations * Subject is in generally good health and has a current Panelist Profile Form on file at ECRL * Subject agrees to sign a Photography Release Form, providing consent for the capture of digital images for use in relation to this clinical study * Subject has completed a HIPAA Authorization Form in conformance with 45 CFR Parts 160 and 164 * Subject understands and has signed an Informed Consent Form in conformance with 21 CFR Part 50: "Protection of Human Subjects." Exclusion Criteria * Female subject is pregnant, nursing, planning a pregnancy, or not using adequate birth control * Subject has been part of a clinical test for a LED device, microcurrent device or other facial device within the last 6 months * Subject has eye sensitivity to light that may interfere with the use/application of the test product * Subject has received treatment with sympathomimetics, antihistamines, vasoconstrictors, non-steroidal anti-inflammatory agents, and/or systemic or topical corticosteroids within one week prior to initiation of the study * Subject has a history of acute or chronic dermatologic, medical, and/or physical conditions which would, in the opinion of the Principal Investigator, preclude application of the test material and/or could influence the outcome of the study * Subject has a history of atopic eczema, psoriasis, or onychomycosis * Subject chronically uses substances such as alcohol, tobacco, recreational drugs, etc. * Subject is currently taking certain medications which, in the opinion of the Principal Investigator, may interfere with the study * Subject exhibits any facial tattoos/tattooed cosmetics, eyelash extensions, rashes, scratches, scars, or burn marks on the test site (face) which may interfere with the study * Subject has known allergies to skin treatment products or cosmetics, toiletries, and/or topical drugs * Subject is unable to communicate or cooperate with the Principal Investigator, language problems, etc. * Subject is on another study utilizing the same test sites (Face) * Subject is an employee of testing firms/laboratories, cosmetic or raw goods manufacturers or suppliers * Subject has any planned medical or cosmetic procedures planned during the course of the study that, at the discretion of the Principal Investigator, may interfere with the study * Subject has a history of skin cancer, or is currently undergoing treatment for active cancer of any kind * Subject has diabetes.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Eurofins CRL Cosmetics, Inc

    Piscataway, New Jersey, 08854, United States

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